# Guangzhou Wondfo Biotech Co., Ltd. – FDA Inspection, Mar 27, 2009

Source: https://www.keypedia.com/records/fda_inspections/guangzhou-wondfo-biotech-co-ltd/97475c23-5a43-4909-83fe-93b3d5db8187
Source feed: FDA_Inspections

> FDA inspection 575291 of Guangzhou Wondfo Biotech Co., Ltd., March 27, 2009. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 575291
- Company Name: Guangzhou Wondfo Biotech Co., Ltd.
- Inspection Date: 2009-03-27
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1108594 - 2018-11-02](https://www.keypedia.com/records/fda_inspections/guangzhou-wondfo-biotech-co-ltd/3903be1a-2a02-4947-9708-087924d6b68a)
- FDA Inspection 877770 - 2014-04-11

Company: https://www.keypedia.com/companies/guangzhou-wondfo-biotech-co-ltd/f821880b-103a-41bf-aebe-4b31ec7e9a9e

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7